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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM01397ZNF467lungMESH:D006457Hemoglobinuria, Paroxysmal
HM01397ZNF467lungMESH:D015428Myocardial Reperfusion Injury
HM01397ZNF467lungMESH:D017029Epilepsy, Complex Partialmuscle
HM01397ZNF467lungMESH:D009402Nephrosis, Lipoidkidney
HM01397ZNF467lungMESH:D003876Dermatitis, Atopicskin
HM01397ZNF467lungMESH:D004827Epilepsymuscle
HM01397ZNF467lungMESH:D012640Seizuresmuscle
HM01397ZNF467lungMESH:D019465Craniofacial Abnormalities
HM01397ZNF467lungMESH:D009369Neoplasmsspleen
HM01397ZNF467lungMESH:D009369Neoplasmsbone marrow
HM01397ZNF467lungMESH:D014178Translocation, Genetic
HM01397ZNF467lungMESH:D012208Rhabdomyosarcomarectum
HM01397ZNF467lungMESH:D012208Rhabdomyosarcomaprostate
HM01397ZNF467lungMESH:D012208Rhabdomyosarcomamuscle
HM01397ZNF467lungMESH:D017563Lung Diseases, Interstitiallung
HM01397ZNF467lungMESH:D011565Psoriasisskin
HM01397ZNF467lungMESH:D006973Hypertensionlung
HM01397ZNF467lungMESH:D006973Hypertensionheart
HM01397ZNF467lungMESH:D006973Hypertensionblood vessel
HM01397ZNF467lungMESH:D018248Adenoma, Liver Cell
HM01397ZNF467lungMESH:D005355Fibrosis
HM01397ZNF467lungMESH:D007674Kidney Diseasesureter
HM01397ZNF467lungMESH:D007674Kidney Diseasespituitary
HM01397ZNF467lungMESH:D007674Kidney Diseaseskidney
HM01397ZNF467lungMESH:D015427Reperfusion Injury
HM01397ZNF467lungMESH:D000015Abnormalities, Multiple
HM01397ZNF467lungMESH:D004828Epilepsies, Partialmuscle
HM01397ZNF467lungMESH:D004832Epilepsy, Absencemuscle
HM01397ZNF467lungMESH:D016135Spinal Dysraphismspinal cord
HM01397ZNF467lungMESH:D020194Unverricht-Lundborg Syndromemuscle
HM01397ZNF467lungMESH:D001778Blood Coagulation Disordersbone marrow
HM01397ZNF467lungMESH:D005317Fetal Growth Retardation
HM01397ZNF467lungMESH:D006333Heart Failureheart
HM01397ZNF467lungMESH:D006943Hyperglycemia
HM01397ZNF467lungMESH:D013226Status Epilepticusmuscle
HM01397ZNF467lungMESH:D013226Status Epilepticusmuscle
HM01397ZNF467lungMESH:D013226Status Epilepticusmuscle
HM01397ZNF467lungMESH:D055371Acute Lung Injury
HM01397ZNF467lungMESH:D005315Fetal Diseases
HM01397ZNF467lungMESH:D006529Hepatomegaly
HM01397ZNF467lungMESH:D002779Cholestasisliver
HM01397ZNF467lungMESH:D005885Gingival Hyperplasia
HM01397ZNF467lungMESH:D000014Abnormalities, Drug-Induced
HM01397ZNF467lungMESH:D006849Hydrocephalusbrain
HM01397ZNF467lungMESH:D014985Xerophthalmiaeye
HM01397ZNF467lungMESH:D004421Dystonia
HM01397ZNF467lungMESH:D019310Pseudolymphoma
HM01397ZNF467lungMESH:D000550Amblyopiabrain
HM01397ZNF467lungMESH:D000550Amblyopiabrain
HM01397ZNF467lungMESH:D005234Fatty Liver
HM01397ZNF467lungMESH:D009404Nephrotic Syndromekidney
HM01397ZNF467lungMESH:D014564Urogenital Abnormalities
HM01397ZNF467lungMESH:D001008Anxiety Disorders
HM01397ZNF467lungMESH:D009139Musculoskeletal Abnormalities
HM01397ZNF467lungMESH:D009190Myelodysplastic Syndromes
HM01397ZNF467lungMESH:D014605Uveitiseye
HM01397ZNF467lungMESH:D015470Leukemia, Myeloid, Acutebone marrow
HM01397ZNF467lungMESH:D009203Myocardial Infarctionheart
HM01397ZNF467lungMESH:D009436Neural Tube Defects
HM01397ZNF467lungMESH:D001714Bipolar Disorder
HM01397ZNF467lungMESH:D012559Schizophrenia
HM01397ZNF467lungMESH:D009765Obesity
HM01397ZNF467lungMESH:D007333Insulin Resistance
HM01397ZNF467lungMESH:D008106Liver Cirrhosis, Experimental
HM01397ZNF467lungMESH:D008881Migraine Disordersbrain
HM01397ZNF467lungMESH:D007638Keratoconjunctivitis Siccaeye
HM01397ZNF467lungMESH:D009135Muscular Diseasesmuscle
HM01397ZNF467lungMESH:D004830Epilepsy, Tonic-Clonicmuscle
HM01397ZNF467lungMESH:D004487Edema
HM01397ZNF467lungMESH:D008113Liver Neoplasms
HM01397ZNF467lungMESH:D008113Liver Neoplasms
HM01397ZNF467lungMESH:D001848Bone Diseases, Developmental
HM01397ZNF467lungMESH:D004831Epilepsies, Myoclonicmuscle
HM01397ZNF467lungMESH:D001321Autistic Disorder
HM01397ZNF467lungMESH:D056486Drug-Induced Liver Injury
HM01397ZNF467lungMESH:D008664Metal Metabolism, Inborn Errorsskin
HM01397ZNF467lungMESH:D008664Metal Metabolism, Inborn Errorsmuscle
HM01397ZNF467lungMESH:D008664Metal Metabolism, Inborn Errorsliver
HM01397ZNF467lungMESH:D008664Metal Metabolism, Inborn Errorskidney